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| Оцветяване с ализариново червено× | Анализ на живи/мъртви клетки× | |
|---|---|---|
| Област | Биоматериали | Биоматериали |
| Семейство | Process / pipeline | Process / pipeline |
| Година на възникване≠ | 2004 | 2000 |
| Създател≠ | Gregory, Gunn, Peister | Invitrogen/Molecular Probes |
| Тип≠ | Staining assay | Dual-dye viability assay |
| Основополагащ източник≠ | Gregory, C. A., Gunn, W. G., Peister, A., & Prockop, D. J. (2004). An Alizarin red-based assay of mineralization by adherent cells in culture: comparison with cetylpyridinium chloride extraction. Analytical Biochemistry, 329(1), 77-84. DOI ↗ | Molecular Probes (2004). LIVE/DEAD Viability/Cytotoxicity Kit user guide. Invitrogen Corporation. link ↗ |
| Други названия | alizarin red-S, calcium staining, bone mineralization assay | calcein-AM/propidium iodide, SYTO/PI staining, fluorescent viability stain |
| Свързани | 4 | 4 |
| Резюме≠ | Alizarin red-S (1,2-dihydroxyanthraquinone-3-sulfonic acid) is a calcium-binding dye that forms a colored complex with mineralized deposits, enabling direct visualization and quantification of bone matrix mineralization. Developed as a standard assay by Gregory and colleagues in 2004, alizarin red staining is widely used to evaluate osteogenic differentiation of stem cells, assess the mineralization-promoting effects of biomaterial scaffolds and growth factors, and measure the calcium content of bone tissue and engineered constructs. The assay is rapid, quantitative, and provides both visual and colorimetric readout. | The Live/Dead assay is a fluorescence-based method for simultaneously identifying live and dead cells using two complementary dyes. The assay combines calcein-AM (or SYTO fluorophores), which generates bright green fluorescence in living cells with intact esterase activity, with propidium iodide (PI), which produces red fluorescence in dead cells with compromised membrane integrity. Commercially developed by Molecular Probes and now part of Thermo Fisher's portfolio, the Live/Dead kit is widely used to evaluate cell viability on biomaterial scaffolds, in tissue constructs, and following drug or toxin exposure. |
| ScholarGateНабор от данни ↗ |
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